Term: Myopia 21, Autosomal Dominant; MYP21
OMIM ID: 614167

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene	Human Gene		Characteristics of this human disease are associated with mutations in...
Zfp644 ZNF644			...the human gene.      MGI data currently do not associate this disease with mutations in the orthologous mouse gene.